Fc receptor homolog 3 is a novel immunoregulatory marker of marginal zone and B1 B cells

Journal of Immunology

Volumn 177, Issue 10, 2006, Pages 6815-6823

  Won, Woong Jai ^a,c   Foote, Jeremy B ^a,c   Odom, Mary R ^a,c   Pan, Jicun ^a,d   Kearney, John F ^a,c   Davis, Randall S ^a,b,c,d  

^a The University of Alabama at Birmingham   (United States)

^b University of Alabama at Birmingham   (United States)

^c University of Alabama at Birmingham   (United States)

^d University of Alabama at Birmingham   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

B LYMPHOCYTE RECEPTOR; BIOLOGICAL MARKER; CALCIUM; CELL PROTEIN; COMPLEMENTARY DNA; FC RECEPTOR; FC RECEPTOR HOMOLOG 3; IMMUNOGLOBULIN; MEMBRANE PROTEIN; MONOCLONAL ANTIBODY; PERVANADATE; TYROSINE; TYROSINE BASED ACTIVATION LIKE PROTEIN; TYROSINE BASED INHIBITORY PROTEIN; UNCLASSIFIED DRUG;

ALLELE; ANIMAL CELL; ARTICLE; B LYMPHOCYTE; BONE MARROW CELL; CALCIUM MOBILIZATION; CELL LINEAGE; CONTROLLED STUDY; DNA DETERMINATION; GENE EXPRESSION; GENETIC CODE; GERMINAL CENTER; IMMUNOREGULATION; MOUSE; MOUSE STRAIN; NONHUMAN; PRE B LYMPHOCYTE; PRIORITY JOURNAL; PROTEIN MOTIF; PROTEIN PHOSPHORYLATION; SEQUENCE ANALYSIS; SEQUENCE HOMOLOGY; SPLEEN CELL;

EID: 33750821382     PISSN: 00221767     EISSN: None     Source Type: Journal    
DOI: 10.4049/jimmunol.177.10.6815     Document Type: Article

References (62)

1. Kraal, G. 1992. Cells in the marginal zone of the spleen. Int. Rev. Cytol. 132: 31-74.
2. Martin, F., and J. F. Kearney. 2002. Marginal-zone B cells. Nat. Rev. Immunol. 2: 323-335.
3. H81X transgene-bearing B cells in fetus and adult: sites for expansion and deletion in conventional and CD5/B1 cells. Int. Immunol. 9: 493-505.
4. Martin, F., and J. F. Kearney. 2000. Positive selection from newly formed to marginal zone B cells depends on the rate of clonal production, CD19, and btk. Immunity 12: 39-49.
5. Kouskoff, V., G. Lacaud, and D. Nemazee. 2000. T cell-independent rescue of B lymphocytes from peripheral immune tolerance. Science 287: 2501-2503.
6. Morse, H. C., III, J. F. Kearney, P. G. Isaacson, M. Carroll, T. N. Fredrickson, and E. S. Jaffe. 2001. Cells of the marginal zone-origins, function and neoplasia. Leak. Res. 25: 169-178.
7. high lymphocytes enriched in the splenic marginal zone generate effector cells more rapidly than the bulk of follicular B cells. J. Immunol. 162: 7198-7207.
8. Song, H., and J. Cerny. 2003. Functional heterogeneity of marginal zone B cells revealed by their ability to generate both early antibody-forming cells and germinal centers with hypermutation and memory in response to a T-dependent antigen. J. Exp. Med. 198: 1923-1935.
9. Kumararatne, D. S., H. Bazin, and I. C. MacLennan. 1981. Marginal zones: the major B cell compartment of rat spleens. Eur. J. Immunol. 11: 858-864.
10. Dunn-Walters, D. K., P. G. Isaacson, and J. Spencer. 1995. Analysis of mutations in immunoglobulin heavy chain variable region genes of microdissected marginal zone (MGZ) B cells suggests that the MGZ of human spleen is a reservoir of memory B cells. J. Exp. Med. 182: 559-566.
11. Tierens, A., J. Delabie, L. Michiels, P. Vandenberghe, and C. Wolf-Peeters. 1999. Marginal-zone B cells in the human lymph node and spleen show somatic hypermutations and display clonal expansion. Blood 93: 226-234.
12. Shih, T. A., E. Meffre, M. Roederer, and M. C. Nussenzweig. 2002. Role of BCR affinity in T cell dependent antibody responses in vivo. Nat. Immunol. 3: 570-575.
13. Pape, K.A., V. Kouskoff, D. Nemazee, H. L. Tang, J. G. Cyster, L. E. Tze, K. L. Hippen, T. W. Behrens, and M. K. Jenkins. 2003. Visualization of the genesis and fate of isotype-switched B cells during a primary immune response. J. Exp. Med. 197: 1677-1687.
14. Vinuesa, C. G., D. M. Sze, M. C. Cook, K. M. Toellner, G. G. Klaus, J. Ball, and I. C. MacLennan. 2003. Recirculating and germinal center B cells differentiate into cells responsive to polysaccharide antigens. Eur. J. Immunol. 33: 297-305.
15. Martin, F., and J. F. Kearney. 2000. B-cell subsets and the mature preimmune repertoire: marginal zone and B1 B cells as part of a "natural immune memory". Immunol. Rev. 175: 70-79.
16. Martin, F., and J. F. Kearney. 2001. B1 cells: similarities and differences with other B cell subsets. Curr. Opin. Immunol. 13: 195-201.
17. Hayakawa, K., R. R. Hardy, D. R. Parks, and L. A. Herzenberg. 1983. The "Ly-1 B" cell subpopulation in normal immunodefective, and autoimmune mice. J. Exp. Med. 157: 202-218.
18. + B cells. Immunol. Rev. 137: 91-118.
19. + B lymphocytes. Int. Immunol. 1: 515-520.
20. Wortis, H. H., and R. Berland. 2001. Cutting edge commentary: origins of B-1 cells. J. Immunol. 166: 2163-2166.
21. Herzenberg, L. A. 2000. B-1 cells: the lineage question revisited. Immunol. Rev. 175: 9-22.
22. Wardemann, H., T. Boehm, N. Dear, and R. Carsetti. 2002. B-1a B cells that link the innate and adaptive immune responses are lacking in the absence of the spleen. J. Exp. Med. 195: 771-780.
23. Alugupalli, K. R., J. M. Leong, R. T. Woodland, M. Muramatsu, T. Honjo, and R. M. Gerstein. 2004. B1b lymphocytes confer T cell-independent long-lasting immunity. Immunity 21: 379-390.
24. Haas, K. M., J. C. Poe, D. A. Steeber, and T. F. Tedder. 2005. B-1a and B-1b cells exhibit distinct developmental requirements and have unique functional roles in innate and adaptive immunity to S. pneumoniae. Immunity 23: 7-18.
25. Radtke, F., A. Wilson, S. J. Mancini, and H. R. MacDonald. 2004. Notch regulation of lymphocyte development and function. Nat. Immunol. 5: 247-253.
26. Guinamard, R., M. Okigaki, J. Schlessinger, and J. V. Ravetch. 2000. Absence of marginal zone B cells in Pyk-2-deficient mice defines their role in the humoral response. Nat. Immunol. 1: 31-36.
27. Girkontaite, I., K. Missy, V. Sakk, A. Harenberg, K. Tedford, T. Potzel, K. Pfeffer, and K. D. Fischer. 2001. Lsc is required for marginal zone B cells, regulation of lymphocyte motility and immune responses. Nat. Immunol. 2: 855-862.
28. Zinkernagel, R. M., S. Ehl, P. Aichele, S. Gehen, T. Kundig, and H. Hengartner. 1997. Antigen localisation regulates immune responses in a dose- and time-dependent fashion: a geographical view of immune reactivity. Immunol. Rev. 156: 199-209.
29. Won, W. J., and J. F. Kearney. 2002. CD9 is a unique marker for marginal zone B cells, B1 cells, and plasma cells in mice. J. Immunol. 168: 5605-5611.
30. Davis, R. S., Y. H. Wang, H. Kubagawa, and M. D. Cooper. 2001. Identification of a family of Fc receptor homologs with preferential B cell expression. Proc. Natl. Acad. Sci. USA 98: 9772-9777.
31. Davis, R. S., G. R. Ehrhardt, C. M. Leu, M. Hirano, and M. D. Cooper. 2005. An extended family of Fc receptor relatives. Eur. J. Immunol. 35: 674-680.
32. Leu, C. M., R. S. Davis, L. A. Gartland, W. D. Fine, and M. D. Cooper. 2005. FcRH1: an activation coreceptor on human B cells. Blood 105: 1121-1126.
33. Ehrhardt, G. R., R. S. Davis, J. T. Hsu, C. M. Leu, A. Ehrhardt, and M. D. Cooper. 2003. The inhibitory potential of Fc receptor homolog 4 on memory B cells. Proc. Natl. Acad. Sci. USA 100: 13489-13494.
34. Davis, R. S., G. Dennis, Jr., M. R. Odom, A. W. Gibson, R. P. Kimberly, P. D. Burrows, and M. D. Cooper. 2002. Fc receptor homologs: newest members of a remarkably diverse Fc receptor gene family. Immunol. Rev. 190: 123-136.
35. Davis, R. S., R. P. Stephan, C. C. Chen, G. Dennis, Jr., and M. D. Cooper. 2004. Differential B cell expression of mouse Fc receptor homologs. Int. Immunol. 16: 1343-1353.
36. Alder, M. N., I. B. Rogozin, L. M. Iyer, G. V. Glazko, M. D. Cooper, and Z. Pancer. 2005. Diversity and function of adaptive immune receptors in a jawless vertebrate. Science 310: 1970-1973.
37. Kearney, J. F., A. Radbruch, B. Liesegang, and K. Rajewsky. 1979. A new mouse myeloma cell line that has lost immunoglobulin expression but permits the construction of antibody-secreting hybrid cell lines. J. Immunol. 123: 1548-1550.
38. Oliver, A. M., F. Martin, and J. F. Kearney. 1997. Mouse CD38 is down-regulated on germinal center B cells and mature plasma cells. J. Immunol. 158: 1108-1115.
39. Altschul, S. F., W. Gish, W. Miller, E. W. Myers, and D. J. Lipman. 1990. Basic local alignment search tool. J. Mol. Biol. 215: 403-410.
40. Kimberly, R. P., J. E. Salmon, and J. C. Edberg. 1995. Receptors for immunoglobulin G: molecular diversity and implications for disease. Arthritis Rheum. 38: 306-314.
41. Wilson, M. J., M. Torkar, A. Haude, S. Milne, T. Jones, D. Sheer, S. Beck, and J. Trowsdale. 2000. Plasticity in the organization and sequences of human KIR/ILT gene families. Proc. Natl. Acad. Sci. USA 97: 4778-4783.
42. Cariappa, A., M. Tang, C. Parng, E. Nebelitskiy, M. Carroll, K. Georgopoulos, and S. Pillai. 2001. The follicular versus marginal zone B lymphocyte cell fate decision is regulated by Aiolos, Btk, and CD21. Immunity 14: 603-615.
43. Saito, T., S. Chiba, M. Ichikawa, A. Kunisato, T. Asai, K. Shimizu, T. Yamaguchi, G. Yamamoto, S. Seo, K. Kumano, et al. 2003. Notch2 is preferentially expressed in mature B cells and indispensable for marginal zone B lineage development. Immunity 18: 675-685.
44. Loder, F., B. Mutschler, R. J. Ray, C. J. Paige, P. Sideras, R. Torres, M. C. Lamers, and R. Carsetti. 1999. B cell development in the spleen takes place in discrete steps and is determined by the quality of B cell receptor-derived signals. J. Exp. Med. 190: 75-89.
45. Srivastava, B., W. J. Quinn, III, K. Hazard, J. Erikson, and D. Allman. 2005. Characterization of marginal zone B cell precursors. J. Exp. Med. 202: 1225-1234.
46. high B cells: a population of mixed origin. Eur. J. Immunol. 29: 3285-3294.
47. Wang, Y., S. R. Brooks, X. Li, A. N. Anzelon, R. C. Rickert, and R. H. Carter. 2002. The physiologic role of CD19 cytoplasmic tyrosines. Immunity 17: 501-514.
48. Amsbaugh, D. F., C. T. Hansen, B. Prescott, P. W. Stashak, D. R. Barthold, and P. J. Baker. 1972. Genetic control of the antibody response to type 3 pneumococcal polysaccharide in mice. I. Evidence that an X-linked gene plays a decisive role in determining responsiveness. J. Exp. Med. 136: 931-949.
49. Hayakawa, K., R. R. Hardy, and L. A. Herzenberg. 1986. Peritoneal Ly-1 B cells: genetic control, autoantibody production, increased λ light chain expression. Eur. J. Immunol. 16: 450-456.
50. Rickert, R. C., K. Rajewsky, and J. Roes. 1995. Impairment of T-cell-dependent B-cell responses and B-1 cell development in CD19-deficient mice. Nature 376: 352-355.
51. Engel, P., L. J. Zhou, D. C. Ord, S. Sato, B. Koller, and T. F. Tedder. 1995. Abnormal B lymphocyte development, activation, and differentiation in mice that lack or overexpress the CD19 signal transduction molecule. Immunity 3: 39-50.
52. Oliver, A. M., F. Martin, G. L. Gartland, R. H. Carter, and J. F. Kearney. 1997. Marginal zone B cells exhibit unique activation, proliferative and immunoglobulin secretory responses. Eur. J. Immunol. 27: 2366-2374.
53. Storb, U., C. Pinkert, B. Arp, P. Engler, K. Gollahon, J. Manz, W. Brady, and R. L. Brinster. 1986. Transgenic mice with μ and κ genes encoding antiphosphorylcholine antibodies. J. Exp. Med. 164: 627-641.
54. Guselnikov, S. V., A. Erilova, A. M. Najakshin, N. Cohen, J. Robert, and A. V. Taranin. 2004. FcR-like genes in the amphibian xenopus: species-specific expansion, structural diversity, and developmental expression. In 12th International Congress on Immunology and 4th Annual Conference FOCIS, July 18-23. Montreal, Quebec, Canada, Abstract 4726.
55. Allman, D., R. C. Lindsley, W. DeMuth, K. Rudd, S. A. Shinton, and R. R. Hardy. 2001. Resolution of three nonproliferative immature splenic B cell subsets reveals multiple selection points during peripheral B cell maturation. J. Immunol. 167: 6834-6840.
56. Cariappa, A., T. Shoham, H. Liu, S. Levy, C. Boucheix, and S. Pillai. 2005. The CD9 tetraspanin is not required for the development of peripheral B cells or for humoral immunity. J. Immunol. 175: 2925-2930.
57. Xu, M. J., R. Zhao, H. Cao, and Z. J. Zhao. 2002. SPAP2, an Ig family receptor containing both ITIMs and ITAMs. Biochem. Biophys. Res. Commun. 293: 1037-1046.
58. Morris, D. L., and T. L. Rothstein. 1994. Decreased surface IgM receptor-mediated activation of phospholipase C γ 2 in B-1 lymphocytes. Int. Immunol. 6: 1011-1016.
59. Chumley, M. J., J. M. Dal Porto, and J. C. Cambier. 2002. The unique antigen receptor signaling phenotype of B-1 cells is influenced by locale but induced by antigen. J. Immunol. 169: 1735-1743.
60. Pillai, S., A. Cariappa, and S. T. Moran. 2005. Marginal zone B cells. Annu. Rev. Immunol. 23: 161-196.
61. Wen, L., J. Brill-Dashoff, S. A. Shinton, M. Asano, R. R. Hardy, and K. Hayakawa. 2005. Evidence of marginal-zone B cell-positive selection in spleen. Immunity 23: 297-308.
62. Maltais, L. J., R. C. Lovering, A. V. Taranin, M. Colonna, J. V. Ravetch, R. Dalla-Favera, P. D. Burrows, M. D. Cooper, and R. S. Davis. 2006 New nomenclature for Fc receptor-like molecules. Nat. Immunol. 7: 431-432.